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Healthcare
› Pharmacovigilance
Pharmacovigilance
354 open positions
Associate Director, Clinical Trial Patient Safety
AbbVie
North Chicago, IL, us
today
Manage worldwide surveillance of clinical trial patient safety data, ensuring compliant and timely adverse event monitoring and review for assigned compound studies.
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Senior Medical Director, Immunology, Global Patient Safety
AbbVie
North Chicago, IL, us
today
Lead global patient safety and pharmacovigilance activities for immunology products, ensuring safety through surveillance, signal detection, and risk management.
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Associate Director, Quality Auditor, GVP
Gsk
Remote
1d
Lead independent global pharmacovigilance audits and drive quality compliance strategies across R&D to ensure adherence to international regulations and GSK standards.
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Senior PV Officer
Ergomed
Pune, MH, in
1d
Senior Pharmacovigilance Officer managing Individual Case Safety Reports (ICSRs), safety data reconciliation, and acting as Local Contact Person for Pharmacovigilance (LCPPV) and Person Responsible for Local Screening (PRLS) for specific countries/languages.
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Senior Scientist, Risk Management & Safety Surveillance
Jobgether
Remote
$80k–$80k
1d
Leading pharmacovigilance activities to assess medicine safety and benefit-risk profiles, including aggregate safety reports, signal evaluation, and regulatory responses.
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Associate Regulatory Affairs Quality, Standards & Training Director (Global Patient Safety )
Jobgether
Remote
$163k–$163k
1d
Provides compliance oversight across Global Patient Safety and Regulatory Affairs, monitoring indicators, inspection-readiness, and operational performance for clinical programs.
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Senior Director of ICSR
Ergomed
Belgrade, rs
1d
Manages the ICSR Management Unit, overseeing staff, resources, and processes to ensure high-quality pharmacovigilance case processing and productivity.
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Senior Director of ICSR
Ergomed
Zagreb, hr
1d
Manages the ICSR Management Unit, overseeing staff, resources, and processes to ensure high-quality pharmacovigilance case processing and patient safety reporting.
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Pharmacovigilance Specialist
Iqvia
Remote
2d
Review, assess, and process safety data and information across service lines, including collecting and tracking incoming Adverse Events (AEs), database entry, coding, and writing narratives.
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Medical Director/Senior Medical Director - Endocrinology(Remote U.S)
↗
Thermo Fisher Scientific
Remote
$200k–$200k
2d
Provides medical oversight of clinical trials to ensure safety profiles, regulatory compliance, and accurate medical content for new drug development.
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PV Coordinator
Thermofisher
Remote, Bulgaria
2d
Lead project coordination and safety support for global and domestic clinical programs, focusing on adverse events, protocol inquiries, and Data and Safety Monitoring Boards.
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Global Patient Safety and Pharmacovigilance Industrial Placement, UK 2027
Gsk
UK – London – New Oxford Street
$29k–$29k
2d
Support Global Safety teams in monitoring medicine safety, collecting and analyzing adverse event data, and assisting in benefit-risk assessments for clinical trials and post-marketing.
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Patient Safety PVSci Manager
Vrtx
Remote
$121k–$121k
2d
Leads pharmacovigilance science activities including cross-functional safety data monitoring, aggregate reporting to regulatory agencies, and signal/risk management for assigned products.
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Scientific Director, Immunology, Global Patient Safety
AbbVie
North Chicago, IL, us
2d
Leads the development and implementation of safety strategies for immunology assets throughout the drug lifecycle, ensuring medical accuracy and scientific rigor in regulatory and clinical documents.
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Senior Benefit/Risk Associate
Ergomed
Belgrade, rs
2d
Performing and supporting contracted pharmacovigilance activities, specifically signal detection, evaluation, and reporting to ensure patient safety.
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Specialist, Drug Safety
Msd
EGY - Cairo - Cairo (New Cairo), EG
3d
Manage pharmacovigilance intake, prepare and submit Individual Case Safety Reports (ICSRs) and aggregate safety reports, and support audits/inspections to ensure regulatory compliance and patient safety across the Middle East.
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Medical Director/Senior Medical Director - Endocrinology(Remote U.S)
Thermofisher
Remote
$200k–$200k
3d
Provides medical oversight of clinical trials to ensure safety profiles, regulatory compliance, and accurate medical content for drug development.
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Medical Information Specialist I - Nurse
Thermofisher
Morrisville, North Carolina, USA
3d
Provide technical and medical information, intake adverse events, and manage product complaints for pharmaceutical and device products.
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FSP Pharmacovigilance Coordinator (Night Shift)
Thermofisher
Remote, Philippines
3d
Coordinate pharmacovigilance safety support and project management for global and domestic clinical programs, managing adverse events, DSMB/EAC meetings, and contractual documentation.
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Lead Pharmacist Contact Center Specialist
Denverhealth
Rocky Mountain Poison & Drug Safety - 1391 Speer Blvd, Denver, CO 80204, US
$110k–$110k
3d
Provides medical information, collects safety reports, and manages product complaints for consumers, patients, and healthcare providers.
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Medical Project Coordinator
Thermofisher
Remote, Serbia, BR
3d
Coordinate and review safety data, monitor clinical trial safety trends, and ensure compliance with regulatory standards to support drug safety operations.
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Senior PV Associate
Ergomed
Sofia, Sofia City Province, bg
3d
Managing Individual Case Safety Reports (ICSRs) and safety data for pharmaceutical and biotechnology clients.
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Senior Scientist, Risk Management & Safety Surveillance
ClinChoice
Canada
3d
Senior scientist responsible for aggregate safety reports, case-level reviews, and safety strategy development for pharmaceutical products.
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Senior Associate, Aggregate Reporting Physician
ClinChoice
Philippines - Pasig
4d
Guide report strategy and review medical/safety content (signals, adverse events, benefit-risk assessments) for pharmaceutical safety reports.
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Administration Copay Assistants (Bilingual - Fluent in French))
Jobgether
Remote
$50k–$50k
4d
Administrative professional supporting drug safety and pharmacovigilance programs by managing clinical and patient information, ensuring safety documentation accuracy, and processing adverse event reports.
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Medical Monitor - CNS
↗
Cognitive Research Corporation
Remote, US
4d
Provide medical, scientific, and safety oversight for clinical trials, ensuring protocol adherence, participant safety, and data integrity.
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Pharmacovigilance associate, Safety data management
↗
Alvotech
KA, IN
4d
Manage clinical safety and post-marketing pharmacovigilance activities including ICSR/SAE management, regulatory submissions, and literature monitoring for biosimilar medicines.
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Senior Patient Safety Physician
↗
Boehringer Ingelheim
Straße, RP, DE
4d
Lead global patient safety strategy and drive benefit-risk assessments for compounds in development and marketed products.
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Senior Manager, Safety Scientist
AstraZeneca
US - Boston - MA
$133k–$133k
4d
Lead global patient safety risk evaluation and management across the product lifecycle, ensuring compliance with GxP and global regulations.
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Senior Medical Director / Medical Director - Endocrinology
↗
Thermo Fisher Scientific
São Paulo, SP, BR
4d
Provide medical oversight of clinical trials and marketed products to ensure regulatory compliance and safety, serving pharmaceutical clients and biotech partners.
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Director/Senior Director - Clinical Safety and Pharmacovigilance
↗
Soterius
UP, IN
4d
Provide strategic and operational leadership for end-to-end pharmacovigilance and clinical safety activities across clinical trial and post-authorization products.
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Associate Safety Case Reviewer
↗
TransPerfect
MH, IN
4d
Analyze and report on safety parameters for clients' products within the context of patient safety, supporting clinical research.
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Temp Mgr Global Patient Safety Sciences
Regeneron
TARRYTOWN, US
4d
Manage global patient safety strategies for molecules in clinical development and post-marketing phases, including safety data aggregation, review, analysis, and benefit-risk assessment.
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Executive Medical Director, SERM
Sarepta
Cambridge, MA
$313k–$313k
4d
Lead safety scientists and physicians to oversee pharmacovigilance, risk management, and safety data analysis for investigational and marketed products in muscle, CNS, and cardiac disease programs.
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Associate Director, Patient Safety Scientist
↗
AstraZeneca
Barcelona, CT, ES
4d
Leads proactive pharmacovigilance and risk management planning, evaluates clinical implications of safety data, and authors regulatory documents for drug safety.
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Associate Director, Patient Safety Scientist
AstraZeneca
Spain - Barcelona
4d
Leads proactive pharmacovigilance and risk management planning, evaluates clinical implications of safety data to establish drug safety profiles, and authors strategic input for regulatory documents.
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Consumer Safety Science Scientist
Gsknch
Warsaw
$145k–$145k
4d
Monitor and evaluate product safety across clinical development and post-marketing settings, ensuring accurate safety information and regulatory compliance.
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Principal Investigator (Virtual)
Careaccess
Remote
$200k–$200k
4d
Provide overall medical oversight and review of clinical trial protocols, safety reports, and case report forms to ensure participant safety and regulatory compliance.
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Principal Investigator
Careaccess
Florida
$200k–$200k
4d
Provide overall medical oversight and review of clinical trial protocols, safety reports, and case report forms to ensure participant safety and regulatory compliance.
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Associate Director. ICSR
Ergomed
Raleigh, NC, us
4d
Managing the ICSR Management Unit, optimizing resource allocation, and leading line managers to ensure productivity in pharmacovigilance operations.
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Case Processing Manager, Team Lead (PV Manager)
Ergomed
Lisbon, Lisbon, pt
4d
Line manages ICSR staff and oversees contracted pharmacovigilance activities, including case processing, quality control, and process optimization.
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Senior Medical Director / Medical Director - Endocrinology
Thermofisher
Remote, Mexico
5d
Provide medical oversight of clinical trials and marketed products to ensure regulatory compliance and safety, serving pharmaceutical clients and research organizations.
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Associate Director, Global Patient Safety Standards & Training
Regeneron
Warren, US
$157k–$157k
5d
Establish and maintain Pharmacovigilance (PV) procedures and policies to ensure global regulatory compliance and operational efficiency.
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Principal Safety Scientist - SERM
Gsk
Remote
$215k–$215k
5d
Provides medical/scientific knowledge in the safety evaluation and risk management of GSK products in clinical development and/or the post-marketing setting.
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Senior Manager, Global Patient Safety - General Medicine
Regeneron
Uxbridge1, GB
5d
Lead scientific safety strategies for molecules in clinical development and post-marketing phases, including data aggregation, review, analysis, and benefit-risk assessment.
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Sr Safety Reporting Specialist
ThermoFisher Scientific
Brasil
6d
Lead and oversee the preparation of complex safety reports, ensure compliance with international pharmacovigilance regulations, and drive continuous improvement in reporting processes to safeguard patient health.
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Executive Director - Clinical Research Physician - GPS Medical
Lilly
São Paulo, Estado de São Paulo
6d
Lead the development, management, and execution of safety programs for therapeutic assets throughout their lifecycle, ensuring proactive pharmacovigilance and risk management.
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Sr Safety Reporting Specialist
Thermo Fisher Scientific
São Paulo, Estado de São Paulo
6d
Lead and oversee the preparation of complex safety reports, ensure compliance with international pharmacovigilance regulations, and drive continuous improvement in reporting processes to safeguard patient health.
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Pharmacovigilance Specialist - NQPPV Backup (Saudi National)
AbbVie
Riyadh, Riyadh Province, sa
7d
Supports the Affiliate Safety Representative and Regional Pharmacovigilance Lead in coordinating and executing affiliate pharmacovigilance activities in Saudi Arabia, ensuring legal, regulatory, quality, and ethical responsibilities for patient safety.
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LOCAL CASE INTAKE ADVISOR
AstraZeneca
Taiwan
8d
Manage the intake, processing, and communication of Individual Case Safety Reports (ICSRs) to safeguard patients and ensure regulatory compliance.
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